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Plasdent

FDA UDI

Class I (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
Plasdent FDA UDI
Generic Name
Dental cheek retractor, professional, single-use FDA UDI
Device Name
Mouth Retractor Ring, Regular FDA UDI
Model / Reference
MUR-M FDA UDI
Description
Mouth Retractor Ring, Regular FDA UDI

Identifiers

Catalog Number
MUR-M FDA UDI
Primary DI / UDI-DI
D832MURM1 FDA UDI
FDA Product Code
EIG FDA UDI
GMDN Term
Dental cheek retractor, professional, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental cheek retractor, professional, single-use

Plasdent by Plasdent Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental cheek retractor, professional, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI 1e3ebbf7-5ee1-4a3e-ba3c-96251a6b0b45 34 fields · synced Jun 8, 2026